The Fluorination of Boron Trichloride - Journal of the American

The Fluorination of Boron Trichloride. Harold Simmons Booth ... Boron Subhalides and Related Compounds with Boron-Boron Bonds. A. K. Holliday and A. G...
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HAROLD SIMMONS BOOTHAND [CONTRIBUTION FROM THE

SPENCER

G . FRARY

VOl. 65

MORLEY CHEMICAL LABORATORY, WESTERN RESERVE UNIVERSITY 1

The Fluorination of Boron Trichloride BY HAROLD SIMMONS BOOTHAND SPENCER G. FRARY This investigation is a continuation of the studies of this Laboratory on the fluorination of nonpolar halides.' Boron trichloride was prepared by the chlorination of ferro-boron.2 The purified boron chloride showed a sharp melting point a t -107' agreeing with the value given by Stock and Priess3 A. The Reaction of Boron Fluoride with Boron Chloride.-Passing a mixture of boron chloride and boron fluoride through a tube heated to 500' caused no rearrangement such as that found by Booth and Bozarth4 with similar mixtures of phosphorus trichloride and fluoride. Exposing the same mixtures to an electric discharge was also without effect. B. Fluorination Using Calcium Fluoride.The fluorination of non-polar halides in the vapor phase by heated calcium fluoride has been used successfully in this Laboratory in the partial fluorination of phosphorus trichloride,* and of phosphoryl chloride." The apparatus consisted of a vertical tube 2 cm. in diameter filled with pellets of calcium fluoride, connected to a rectifying column with a head cooled with liquid ammonia that coiidensed and returned the unreacted boron chloride to an ampoule from which it again circulated through the system. An automatic stopcock which permitted the reaction products to bleed off, while most of the unredcted boron chloride, recircuhted, maintained the system a t the desired pressure of 14.7 cni. of mercury. The first fluorination with calciuiii fluoride heated to 200' produced only boron trifluoride, showing complete fluorination. A second fluoritlation with the pellets at first at room temperature and theii at gradually rising temperature until the reaction started, showed no reaction until the temperature reached 160°, when it proceeded quite rapidly forming only boron trifluoride. Subsequent runs in which the temperature was lowered after the reaction had started also gave boron trifluoride as the sole product. ( I ) Booth and Caseidy, 'l'lrls J O U K N A L , 62, 3 6 ! J ( I ! r l U ) 12) M a z e t t i and de Carli, A l l i .4r,rd. / . i v < ? i , 131 31, ii. 11!1 (LIIW). ( 3 ) Stork and I'ries,, Hfi , 41, : 4 l O ! l 1 1 ! l 1 I). ( I ) n d l l .inil i 3 u m r t l i . 'I H I > J O I ' K Z A I . . 66, :JX!lU (l',l; i i l , 61, L " ! . : i U'!l.;!l)

With fresh calcium fluoride pellets the reaction proceeded very rapidly with almost complete conversion to boron trifluoride on a single pass. As the reaction proceeded the pellets became coated with calcium chloride and the reaction slowed. However, even then there did not seem to be any tendency to form intermediate compounds. C. Fluorination with Antimony Fluoride and a Catalyst.-With the type of generator cominonly used in this a run was made with the mixture, BC13 and SbC16, maintained a t 0' and at approximately half an atmosphere pressure. The generator was cooled with ice while the still-head was a t room temperature. Upon addition of sublimed antimony fluoride, the reaction proceeded smoothly with pure boron trifluoride as the only product obtained. Since lowering the temperature slowed the reaction, it was thought that it might favor the production of the intermediates, so runs were made at -15' using an ice-salt mixture for cooling, at -40' using liquid ammonia and at -78' using a solid carbon dioxide-acetone mixture. While the reaction was slowed proportioiially in these runs, only the completely fluorinated product was obtained. In each of these cases the pressure was adjusted so that a little of the boron chloride could distill over. In this way any intermediate compound that was formed should have escaped immediately and should iiot have had opportunity to be fluorinated further. Dilution of the boron trichloride with a11equal amount of carbon tetrachloride gave only pure BF3. At the teniperature used (-400) none of the carbon tetrachloride was fluorinated while thc boron trichloride was coilverted to the trifluoritle. The fluoriiiatioii is thought to proceed by the forinatioii of a i l xtditioii product of antirnoiiy trifluoricle with t h e halide which in turn deconiposes forming the fluori~iated coinpound and eventually :irrtiuwi\y trichloride. With the thought of rediic.iiig it.; activity, aiitiiiiony fluoride atid trichloride were iiiised together in the molecular proportioils aiitiuioiiy iiioiiofluorodichloridc 'l'his iiiisturc. W;LS usiv1 t o fluorillate i u i t i fuscbtl. II,I

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THEFLUORINATION OF BORON TRICHLORIDE

some boron trichloride but the only effect was to slow the reaction considerably while still giving pure boron trifluoride. Identification of the Fluorination Products.The products obtained from the fluorination were separated by fractional distillation and the various fractions identified by their boiling points and vapor densities according to the standard technique in this Laboratory.'

Discussion of Results The fluorination of boron trichloride by antimony fluoride and pentachloride is decidedly exothermic, and proceeds quite rapidly a t room temperatures and even proceeds, although considerably more slowly, a t -78". Due to the heat evolved (when the reaction starts), there is a tendency for local over-heating that makes the reaction proceed more rapidly. Also the antimony trifluoride that is added is a t room temperature so that it momentarily warms the liquid with which it comes in contact and accelerates the reaction. The theory of Booth and Swinehart8 for the formation of partially fluorinated products assumes that the stability of the compound of the partially fluorinated chloride and the fluorinating agent is so little a t the temperature of the fluorination that dissociation takes place liberating the partially fluorinated chloride as a gas which may be removed to prevent further fluorination. However, BC1, and BF3 are noted for their ability to act as acceptors for electron pairs forming unusually stable compounds. Apparently this bond is so strong that internie( 7 ) Booth and Bozarth, I n d . Ew. Chem., 29, 470 (1937). (8) Booth and Swinehart, THISJOURNAL, I?, 1333, 1337 (1935).

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diate fluorinated products cannot be released. If this explanation is true then fluorination a t elevated temperatures (under pressure) might permit the liberation of partly fluorinated compounds. However, the fact that none were obtained by fluorination by calcium fluoride under carefully controlled conditions, nor by heating or sparking a mixture of BFI and BC13, would suggest that under these higher temperature conditions BFlCl and BFClz rearrange to form BF, and BC& just as Booth and Morris found that on standing even a t -78' C., GeF3C1, GeFzCln and GeFC13 rearranged to GeF4 and GeC14. Boron chloride represents a fourth class of reaction of non-polar halide and antimony trifluoride in the presence of pentavalent antimony in which the degree of covalent unsaturation is so great that no intermediate product can be isolated. Benzotrichl~ride~ likewise is completely fluorinated by this reagent but it is not probable that the reason is the same. Summary The fluorination of boron trichloride by antimony trifluoride with antimony pentachloride as a catalyst a t O', -13', -40°, and -$go, and by calcium fluoride heated to 160 and 200' yielded pure boron trifluoride as the sole fluorination product. This should be a useful laboratory method for preparing BF3 free from SiF4. When mixtures of boron trifluoride and boron trichloride were heated or subjected to electrical discharge, no rearrangement took place. CLEVELAND, OHIO RECEIVED JULY 1, 1943 2066 (1935); Booth and (9) Booth, Elsey and Burchfield, ibid., I?, Burchfield, i b i d . , 67, 2070 (1935).